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Depiction
Upstream Precursor
Thiamine diphosphate
CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCOP(=O)(O)OP(=O)(O)O
Depth 1
Depiction
Product
3-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-4-methyl-5-[2-(phosphonooxy)ethyl]thiazolium
CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCOP(=O)(O)O
Depiction
Precursor
3-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-4-methyl-5-[2-(phosphonooxy)ethyl]thiazolium
CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCOP(=O)(O)O
Depth 2
Depiction
Downstream Successor
2-(4-Methyl-1,3-thiazol-3-ium-5-yl)ethanol
CC1=C(SC=[NH+]1)CCO
Depiction
Precursor
3-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-4-methyl-5-[2-(phosphonooxy)ethyl]thiazolium
CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCOP(=O)(O)O
Depth 3
Depiction
Downstream Successor
2-(4-Methyl-1-oxo-1,3-thiazol-5-yl)ethanol
OCCC1=C(N=CS1=O)C
Depiction
Precursor
3-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-4-methyl-5-[2-(phosphonooxy)ethyl]thiazolium
CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCOP(=O)(O)O
Depth 3
Depiction
Downstream Successor
4-Methyl-5-thiazoleacetaldehyde
CC1=C(SC=N1)CC=O
Depiction
Precursor
3-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-4-methyl-5-[2-(phosphonooxy)ethyl]thiazolium
CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCOP(=O)(O)O
Depth 1
Depiction
Downstream Successor
Thiamine
CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCO
Depiction
Precursor
3-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-4-methyl-5-[2-(phosphonooxy)ethyl]thiazolium
CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCOP(=O)(O)O
Depth 3
Depiction
Downstream Successor
2-[4-Methyl-3-[(2-methyl-4-nitrosopyrimidin-5-yl)methyl]-1,3-thiazol-3-ium-5-yl]ethanol
Cc1c(sc[n+]1Cc2cnc(nc2N=O)C)CCO
Depiction
Precursor
3-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-4-methyl-5-[2-(phosphonooxy)ethyl]thiazolium
CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCOP(=O)(O)O
Depth 3
Depiction
Downstream Successor
Thiamine acetic acid
CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CC(=O)O
No Original Precursors

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